» Articles » PMID: 33573601

Development of a Novel Model of Cholecystectomy in Subsequently Ovariectomized Mice and Characterization of Metabolic and Gastrointestinal Phenotypes: a Pilot Study

Overview
Publisher Biomed Central
Specialty Gastroenterology
Date 2021 Feb 12
PMID 33573601
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Cholecystectomy (XGB) is the most common abdominal surgery performed in the United States and is associated with an increased post-surgery incidence of metabolic and gastrointestinal (GI) diseases. Two main risk factors for XGB are sex (female) and age (40-50 yr), corresponding with onset of menopause. Post-menopausal estrogen loss alone facilitates metabolic dysfunction, but the effects of XGB on metabolic and GI health have yet to be investigated in this population. Study objectives were to (1) identify possible short-term effects of XGB and (2) develop a novel murine model of XGB in human menopause via subsequent ovariectomy (OVX) and assess longitudinal effects of OVX on metabolism, GI physiology, and GI microbiota in XGB mice.

Methods: Female C57BL/6 mice were utilized in two parallel studies (S1&S2). In S1, XGB mice were compared to a non-XGB baseline group after six wk. In S2, mice were XGB at wk0, either sham (SHM) or OVX at wk6, and sacrificed at wk12, wk18, and wk24. Body composition assessment and fresh fecal collections were conducted periodically. Serum and tissues were collected at sacrifice for metabolic and GI health endpoints.

Results: Compared to baseline, XGB increased hepatic CYP7A1 and decreased HMGCR relative expression, but did not influence BW, fat mass, or hepatic triglycerides after six wk. In S2, XGB/OVX mice had greater BW and fat mass than XGB/SHM. Cecal microbiota alpha diversity metrics were lower in XGB/OVX mice at wk24 compared the XGB/SHM. No consistent longitudinal patterns in fasting serum lipids, fecal microbial diversity, and GI gene expression were observed between S2 groups.

Conclusions: In addition to developing a novel, clinically-representative model of XGB and subsequent OVX, our results suggest that OVX resulted in the expected phenotype to some extent, but that XGB may modify or mask some responses and requires further investigation.

Citing Articles

Correlation between cholecystectomy and development of non-alcoholic liver disease in the mouse model.

Kim H, Lee S, Saeed W, Kim H, Oh J, Koh D Ann Transl Med. 2022; 10(15):814.

PMID: 36034996 PMC: 9403915. DOI: 10.21037/atm-21-5414.

References
1.
Wang W, Wang J, Li J, Yan P, Jin Y, Zhang R . Cholecystectomy Damages Aging-Associated Intestinal Microbiota Construction. Front Microbiol. 2018; 9:1402. PMC: 6026649. DOI: 10.3389/fmicb.2018.01402. View

2.
Ure B, Troidl H, Spangenberger W, Lefering R, Dietrich A, Eypasch E . Long-term results after laparoscopic cholecystectomy. Br J Surg. 1995; 82(2):267-70. DOI: 10.1002/bjs.1800820243. View

3.
Caporaso J, Lauber C, Walters W, Berg-Lyons D, Huntley J, Fierer N . Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J. 2012; 6(8):1621-4. PMC: 3400413. DOI: 10.1038/ismej.2012.8. View

4.
Amigo L, Husche C, Zanlungo S, Lutjohann D, Arrese M, Miquel J . Cholecystectomy increases hepatic triglyceride content and very-low-density lipoproteins production in mice. Liver Int. 2010; 31(1):52-64. DOI: 10.1111/j.1478-3231.2010.02361.x. View

5.
Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P . The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 2012; 41(Database issue):D590-6. PMC: 3531112. DOI: 10.1093/nar/gks1219. View